162088-90-6

2'-Nitrophenyl 2,3-di-O-acetyl-4-O-triethylsilyl-β-D-xylopyranoside Chemical Structure
162088-90-6

Chemical Structure

2'-Nitrophenyl 2,3-di-O-acetyl-4-O-triethylsilyl-β-D-xylopyranoside

  • CAS No.: 162088-90-6
  • Formula:C21H31NO9Si
  • Molecular Weight:469.56

IUPAC Name: (2S,3R,4R,5R)-2-(2-nitrophenoxy)-5-((triethylsilyl)oxy)tetrahydro-2H-pyran-3,4-diyl diacetate

InChIKey: BFEHWXCZKFZQCB-MHTWAQMVSA-N

SMILES: CC(O[C@@H]1[C@H]([C@@H](OC[C@H]1O[Si](CC)(CC)CC)OC2=C(C=CC=C2)[N+]([O-])=O)OC(C)=O)=O

Biological Activity: 2'-Nitrophenyl 2,3-di-O-acetyl-4-O-triethylsilyl-β-D-xylopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].

Cat. No. Product Name Purity Description Pricing
HY-W699174
2'-Nitrophenyl 2,3-di-O-acetyl-4-O-triethylsilyl-β-D-xylopyranoside 2'-Nitrophenyl 2,3-di-O-acetyl-4-O-triethylsilyl-β-D-xylopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
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